Bangangxanthone A

Details

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Internal ID e2e77299-ed5f-4cbe-8bc3-c0ca92e79f7c
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones > Pyranoxanthones
IUPAC Name 6,8,11-trihydroxy-3-methyl-3-(4-methylpent-3-enyl)pyrano[2,3-c]xanthen-7-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C23H22O6/c1-12(2)5-4-9-23(3)10-8-13-17(29-23)11-16(26)19-20(27)18-14(24)6-7-15(25)22(18)28-21(13)19/h5-8,10-11,24-26H,4,9H2,1-3H3
InChI Key HFJSQHGZXHTCLI-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C23H22O6
Molecular Weight 394.40 g/mol
Exact Mass 394.14163842 g/mol
Topological Polar Surface Area (TPSA) 96.20 Ų
XlogP 5.30
Atomic LogP (AlogP) 4.97
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

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6,8,11-trihydroxy-3-methyl-3-(4-methylpent-3-enyl)pyrano[2,3-c]xanthen-7-one

2D Structure

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2D Structure of Bangangxanthone A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9847 98.47%
Caco-2 - 0.7653 76.53%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.7059 70.59%
OATP2B1 inhibitior + 0.5671 56.71%
OATP1B1 inhibitior + 0.8767 87.67%
OATP1B3 inhibitior + 0.9528 95.28%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.9303 93.03%
P-glycoprotein inhibitior - 0.4326 43.26%
P-glycoprotein substrate - 0.6539 65.39%
CYP3A4 substrate + 0.5943 59.43%
CYP2C9 substrate - 0.5948 59.48%
CYP2D6 substrate - 0.8144 81.44%
CYP3A4 inhibition - 0.8348 83.48%
CYP2C9 inhibition - 0.5990 59.90%
CYP2C19 inhibition - 0.5823 58.23%
CYP2D6 inhibition - 0.7583 75.83%
CYP1A2 inhibition + 0.5801 58.01%
CYP2C8 inhibition + 0.4526 45.26%
CYP inhibitory promiscuity - 0.5527 55.27%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.6362 63.62%
Eye corrosion - 0.9922 99.22%
Eye irritation - 0.5807 58.07%
Skin irritation - 0.6996 69.96%
Skin corrosion - 0.9314 93.14%
Ames mutagenesis + 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4328 43.28%
Micronuclear - 0.7700 77.00%
Hepatotoxicity + 0.5875 58.75%
skin sensitisation - 0.6771 67.71%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.6161 61.61%
Acute Oral Toxicity (c) III 0.6709 67.09%
Estrogen receptor binding + 0.8828 88.28%
Androgen receptor binding + 0.7192 71.92%
Thyroid receptor binding + 0.7117 71.17%
Glucocorticoid receptor binding + 0.9310 93.10%
Aromatase binding + 0.7834 78.34%
PPAR gamma + 0.8876 88.76%
Honey bee toxicity - 0.8212 82.12%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 0.9688 96.88%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 99.65% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 98.27% 94.45%
CHEMBL2581 P07339 Cathepsin D 95.37% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 94.16% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.15% 89.00%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 92.10% 85.30%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.01% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.83% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.45% 99.17%
CHEMBL3038469 P24941 CDK2/Cyclin A 84.23% 91.38%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 84.21% 83.57%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.77% 90.71%
CHEMBL4208 P20618 Proteasome component C5 83.21% 90.00%
CHEMBL1937 Q92769 Histone deacetylase 2 82.30% 94.75%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 81.67% 89.34%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 81.15% 99.15%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 80.19% 94.80%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
There are no matching plants.

Cross-Links

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PubChem 11524043
LOTUS LTS0199635
wikiData Q105027369